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The Duodenal Mucosa Associated Microbiome, Visceral Sensory Function, Immune Activation and Psychological Comorbidities in Functional Gastrointestinal Disorders with and Without Self-reported Non-celiac Wheat Sensitivity

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Journal Gut Microbes
Date 2022 Oct 28
PMID 36303431
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Abstract

Frequently, patients with functional gastrointestinal disorders (FGIDs) report intolerance of wheat products. We compared gastrointestinal symptoms, sensory function, psychiatric comorbidities, gut-homing immune cells, and duodenal mucosa-associated microbiome (d-MAM) in FGID patients and controls with and without self-reported wheat sensitivity (SR-NCWS). We recruited 40 FGID patients and 20 controls referred by GPs for treatment. Gastrointestinal/extraintestinal symptoms, visceral sensory function, psychological comorbidities, and SR-NCWS were assessed in a standardized approach. Peripheral gut homing T-cells (CD4α4β7CCR9/CD8α4β7CCR9) were quantified, and the d-MAM was assessed by DNA sequencing for 46 subjects. Factors of bacterial genera were extracted utilizing factor analysis with varimax rotation and factors univariately associated with FGID or SR-NCWS included in a subsequent multivariate analysis of variance to identify statistically independent discriminators. Anxiety scores (p < .05) and increased symptom responses to a nutrient challenge (p < .05) were univariately associated with FGID. Gut homing T-cells were increased in FGID patients with SR-NCWS compared to other groups (p all <0.05). MANOVA revealed that anxiety (p = .03), visceral sensory function (p = 0.007), and a d-MAM factor comprise members of the , and lineages were significantly (p = .001) associated with FGID, while gut homing CD4α4 β7CCR9 T-cells were associated (p = .002) with SR-NCWS. Compared to controls, patients with and without SR-NCWS show that there are shifts in the amplicon sequence variants within specific bacterial genera between the FGID subgroups (particularly and ) as well as distinct bacterial taxa discriminatory for the two different FGID subtypes. Compared to controls, both FGID patients with and without SR-NCWS have an increased symptom response to a standardized nutrient challenge and increased anxiety scores. The FGID patients with SR-NCWS - as compared to FGID without SR-NCWS (and controls without SR-NCWS) - have increased gut homing T-cells. The d-MAM profiles suggest species and strain-based variations between the two FGID subtypes and in comparison to controls.

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References
1.
Haag S, Senf W, Tagay S, Heuft G, Gerken G, Talley N . Is there any association between disturbed gastrointestinal visceromotor and sensory function and impaired quality of life in functional dyspepsia?. Neurogastroenterol Motil. 2009; 22(3):262-e79. DOI: 10.1111/j.1365-2982.2009.01415.x. View

2.
Brown G, Hoedt E, Keely S, Shah A, Walker M, Holtmann G . Role of the duodenal microbiota in functional dyspepsia. Neurogastroenterol Motil. 2022; 34(11):e14372. PMC: 9786680. DOI: 10.1111/nmo.14372. View

3.
Rohart F, Gautier B, Singh A, Le Cao K . mixOmics: An R package for 'omics feature selection and multiple data integration. PLoS Comput Biol. 2017; 13(11):e1005752. PMC: 5687754. DOI: 10.1371/journal.pcbi.1005752. View

4.
Koloski N, Jones M, Walker M, Veysey M, Zala A, Keely S . Population based study: atopy and autoimmune diseases are associated with functional dyspepsia and irritable bowel syndrome, independent of psychological distress. Aliment Pharmacol Ther. 2019; 49(5):546-555. DOI: 10.1111/apt.15120. View

5.
Shah A, Gurusamy S, Hansen T, Callaghan G, Talley N, Koloski N . Concomitant Irritable Bowel Syndrome Does Not Influence the Response to Antimicrobial Therapy in Patients with Functional Dyspepsia. Dig Dis Sci. 2021; 67(6):2299-2309. DOI: 10.1007/s10620-021-07149-1. View